A Study of HRS-4508 in Combination With Other Anti-tumor Therapy for Solid Tumor

Recruiting Phase 1 Phase 2 Interventional Study
Solid Tumor
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 75
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
120 (estimated)
Sponsor
Jiangsu HengRui Medicine Co., Ltd. · Industry
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
The study is being conducted to evaluate the efficacy, safety, and ORR of HRS-4508 combination with other anti tumor therapy in subjects with solid tumor ; to evaluate HRS-4508 DLT, MTD and RP2D, to evaluate the incidence and severity of adverse events (AE)/serious adverse events (SAE) (rated based on CTCAE v5.0), to evaluate ORR by researchers based on RECIST v1.1, to evaluate the pharmacokinetic…
Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: 1. Age: 18 to 75 years old; Both men and women are welcome; 2. The mixed cell types need to be confirmed by histology or cytology, and the dominant cell morphology, unresectable or metastatic . 3. ECOG ratings of 0 or 1. 4. Expected survival period ≥ 12 weeks. 5. At least one me…
Contacts

Jiaman Lin

+86 180 0245 4915

jiaman.lin@hengrui.com

CONTACT

Yadan Huo

+86 13381110273

Yadan.huo.yh3@hengrui.com

CONTACT